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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479711Generated: October 30, 2026

Pyridine → HCID 59110594, compound

https://huagongshe.com/reaction/479711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Amino-6-(piperidin-1-ylmethyl)pyridineHCID 18771671—
Reactant5-(4-Carboxy-thiazol-2-yl)-indole-1-carboxylic acid tert-butyl esterHCID 69411139—
SolventTolueneHCID 1140—
ProductHCID 59110594HCID 59110594—

Reaction Steps

To a solution of 5-(4-carboxy-thiazol-2-yl)-indole-1-carboxylic acid tert-butyl ester (2.65 g, 7.69 mmol), molecular sieves, and 100 mL of dry toluene was added TEA (1.6 mL, 11.5 mmol). The resulting solution was stirred for 20 min then DPPA (2.5 mL, 11.6 mmol) was added and the resulting solution was stirred at 80° C. for 40 min. 6-Piperdin-1-ylmethyl-pyridin-2-ylamine (1.64 g, 8.6 mmol) and pyridine (1.0 mL, 12.4 mmol) were added and the mixture was stirred at 80° C. for another 14 h. The molecular sieves were filtered off and washed with CH2Cl2 and MeOH. The filtrate was concentrated in vacuo and the resulting residue was purified by flash chromatography on silica gel using 3% MeOH/CH2Cl2 to give a brown solid. MS m/z: 533 (M+1). Calc'd for C28H32N6O3S-532.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645990B2
Source datasetuspto-grants-2003_11
ORD IDord-4d71ca128932468a87c84388d570bd88
Source noteuspto-grants-2003_11